Encore Medical, L.P.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
81
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K252567AltiVate Reverse® ADLC GlenosphereJanuary 15, 2026
K252974EMPOWR KneeDecember 19, 2025
K251833EMPOWR Acetabular® Liner ExtensionNovember 12, 2025
K252141AltiVate Reverse® GlenoidAugust 5, 2025
K251776EMPOWR Revision Knee™ (EMPOWR Revision VVC+, e+ Tibial Insert)July 8, 2025
K251241EMPOWR Revision Knee™ (EMPOWR Revision Knee™ Symmetric TT Cones)July 2, 2025
K251184AltiVate Reverse Shoulder System; RSP Shoulder System; SMR Shoulder System; PRIMA Humeral System; PRMay 16, 2025
K241483ceramys™ femoral head systemFebruary 7, 2025
K233481AltiVate Reverse® GlenoidMay 29, 2024
K222592AltiVate® Anatomic Shoulder AG e+™ with MarkersJune 23, 2023
K213387AltiVate® Anatomic Shoulder AG e+™ with MarkersJuly 7, 2022
K213793EMPOWR Revision KneeApril 1, 2022
K210308EMPOWR Porous Femur with HAnano SurfaceTMMarch 30, 2021
K203557EMPOWR Dual Mobility Metal Liner, EMPOWR Dual Mobility Poly BearingFebruary 10, 2021
K203026AltiVate® Anatomic Pegged Glenoid with MarkersDecember 23, 2020
K193226AltiVate Anatomic Canal-Sparing (CS) ShoulderJune 3, 2020
K191325EMPOWR Partial KneeJuly 16, 2019
K190057DJO Acetabular SystemJune 7, 2019
K190290AltiVate Reverse Humeral Stem, 48mmApril 26, 2019
K180930EMPOWR VVC TIBIAL INSERTJuly 9, 2018